Magnetic ‘Vaccines’, Nanobots & Bluetooth Signals

Veins Glow After Vaccine Injection


Researchers make magnetic graphene.

Graphene is a one-atom thick sheet of carbon atoms arranged in a hexagonal lattice. UC Riverside physicists have found a way to induce magnetism in graphene while also preserving graphene’s electronic properties. Credit: Shi Lab, UC Riverside.

Graphene, a one-atom thick sheet of carbon atoms arranged in a hexagonal lattice, has many desirable properties. Magnetism alas is not one of them. Magnetism can be induced in graphene by doping it with magnetic impurities, but this doping tends to disrupt graphene’s electronic properties.

Now a team of physicists at the University of California, Riverside has found an ingenious way to induce magnetism in while also preserving graphene’s electronic properties. They have accomplished this by bringing a graphene sheet very close to a magnetic insulator – an electrical insulator with magnetic properties.

“This is the first time that graphene has been made magnetic this way,” said Jing Shi, a professor of physics and astronomy, whose lab led the research. “The magnetic graphene acquires new so that new quantum phenomena can arise. These properties can lead to new electronic devices that are more robust and multi-functional.”

Genetically engineered ‘Magneto’ protein remotely controls brain and behaviour

“Badass” new method uses a magnetised protein to activate brain cells rapidly, reversibly, and non-invasively

The Guardian 24 March, 2016

Researchers in the United States have developed a new method for controlling the brain circuits associated with complex animal behaviours, using genetic engineering to create a magnetised protein that activates specific groups of nerve cells from a distance.

Understanding how the brain generates behaviour is one of the ultimate goals of neuroscience – and one of its most difficult questions. In recent years, researchers have developed a number of methods that enable them to remotely control specified groups of neurons and to probe the workings of neuronal circuits.

The most powerful of these is a method called optogenetics, which enables researchers to switch populations of related neurons on or off on a millisecond-by-millisecond timescale with pulses of laser light. Another recently developed method, called chemogenetics, uses engineered proteins that are activated by designer drugs and can be targeted to specific cell types.

Although powerful, both of these methods have drawbacks. Optogenetics is invasive, requiring insertion of optical fibres that deliver the light pulses into the brain and, furthermore, the extent to which the light penetrates the dense brain tissue is severely limited. Chemogenetic approaches overcome both of these limitations, but typically induce biochemical reactions that take several seconds to activate nerve cells.

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The new technique, developed in Ali Güler’s lab at the University of Virginia in Charlottesville, and described in an advance online publication in the journal Nature Neuroscience, is not only non-invasive, but can also activate neurons rapidly and reversibly.

Several earlier studies have shown that nerve cell proteins which are activated by heat and mechanical pressure can be genetically engineered so that they become sensitive to radio waves and magnetic fields, by attaching them to an iron-storing protein called ferritin, or to inorganic paramagnetic particles. These methods represent an important advance – they have, for example, already been used to regulate blood glucose levels in mice – but involve multiple components which have to be introduced separately.

The new technique builds on this earlier work, and is based on a protein called TRPV4, which is sensitive to both temperature and stretching forces. These stimuli open its central pore, allowing electrical current to flow through the cell membrane; this evokes nervous impulses that travel into the spinal cord and then up to the brain.

Güler and his colleagues reasoned that magnetic torque (or rotating) forces might activate TRPV4 by tugging open its central pore, and so they used genetic engineering to fuse the protein to the paramagnetic region of ferritin, together with short DNA sequences that signal cells to transport proteins to the nerve cell membrane and insert them into it.

When they introduced this genetic construct into human embryonic kidney cells growing in Petri dishes, the cells synthesized the ‘Magneto’ protein and inserted it into their membrane. Application of a magnetic field activated the engineered TRPV1 protein, as evidenced by transient increases in calcium ion concentration within the cells, which were detected with a fluorescence microscope.

Next, the researchers inserted the Magneto DNA sequence into the genome of a virus, together with the gene encoding green fluorescent protein, and regulatory DNA sequences that cause the construct to be expressed only in specified types of neurons. They then injected the virus into the brains of mice, targeting the entorhinal cortex, and dissected the animals’ brains to identify the cells that emitted green fluorescence. Using microelectrodes, they then showed that applying a magnetic field to the brain slices activated Magneto so that the cells produce nervous impulses.

To determine whether Magneto can be used to manipulate neuronal activity in live animals, they injected Magneto into zebrafish larvae, targeting neurons in the trunk and tail that normally control an escape response. They then placed the zebrafish larvae into a specially-built magnetised aquarium, and found that exposure to a magnetic field induced coiling manouvres similar to those that occur during the escape response. (This experiment involved a total of nine zebrafish larvae, and subsequent analyses revealed that each larva contained about 5 neurons expressing Magneto.)

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In one final experiment, the researchers injected Magneto into the striatum of freely behaving mice, a deep brain structure containing dopamine-producing neurons that are involved in reward and motivation, and then placed the animals into an apparatus split into magnetised a non-magnetised sections. Mice expressing Magneto spent far more time in the magnetised areas than mice that did not, because activation of the protein caused the striatal neurons expressing it to release dopamine, so that the mice found being in those areas rewarding. This shows that Magneto can remotely control the firing of neurons deep within the brain, and also control complex behaviours.

Neuroscientist Steve Ramirez of Harvard University, who uses optogenetics to manipulate memories in the brains of mice, says the study is “badass”.

“Previous attempts [using magnets to control neuronal activity] needed multiple components for the system to work – injecting magnetic particles, injecting a virus that expresses a heat-sensitive channel, [or] head-fixing the animal so that a coil could induce changes in magnetism,” he explains. “The problem with having a multi-component system is that there’s so much room for each individual piece to break down.”

“This system is a single, elegant virus that can be injected anywhere in the brain, which makes it technically easier and less likely for moving bells and whistles to break down,” he adds, “and their behavioral equipment was cleverly designed to contain magnets where appropriate so that the animals could be freely moving around.”

‘Magnetogenetics’ is therefore an important addition to neuroscientists’ tool box, which will undoubtedly be developed further, and provide researchers with new ways of studying brain development and function.


Wheeler, M. A., et al. (2016). Genetically targeted magnetic control of the nervous system. Nat. Neurosci., DOI: 10.1038/nn.4265 [Abstract]

Summary of Hydrogel & Quantum Dot Nanotechnology Characteristics


Celeste Solum Former 20 yr FEMA Officer Created this summary based on the information found in dozens of scientific peer reviewed studies and articles.

Mechanical Tooling Robots Force Clamps:Robotic clamps that will forcibly hold synthetic edits into your body structure until they are fused. Pylons: Robotic towers are erected that will be used to bring electrical impulses into your body including the structure used to support the nano particles injecting their payload into your body.

Calipers: Robotic instrument for measuring external or internal dimensions, having two hinged legs resembling a pair of compasses and inturned or outturned points.    Internal locusts anyone?

Information Relays Robots Robotic Networks: Robots whose task will be to connect (link) you with artificial intelligence, people, and things. Nanoactuators: A robotic device for moving or controlling you.

Accordion Racks: Robots with angle comprised of 6by6 meshes (666) controlled by the length of the DNA locks. A. This is a DNA locking system, once they have you where they want you.

Robotic Domino Arrays: A robotic reconfigurable DNA origami domino array (DODA), which is a set of keys (DNA strands) that added to your DNA using cryptographic data. There is an ownership transfer of keys once these arrays are set up. Remember, Jesus holds the keys to life and death.

Nano Medical Robots Robotic Imaging tools: Robotic imaging software is a type of graphic design software inserted into your body that is used to create, edit and manipulate images into your body. Consider, you are created in the Divine Image. Do you want another image in your body?

Robotic Antibody Sensors: Antibodybased robots permit the rapid and sensitive analysis of a range of pathogens and associated toxins and transfer of this data directly to Public Health, from deep inside your body without you ever knowing about it.
Robotic Pliers: Robots with small pincers like a crab for holding small objects or for bending and cutting wire, used in the retooling and rewiring of your body.
Nanorobots: Nanoscopic robots about the size of an atom. Robotic Encapsulation: Robots that are enclosing or sequestering your God given biological processes from the growing hydrogel.
Robotic NanoCages:Robots that 3D chains that cage you. These chains cage your proteins and are tunable to various frequencies.
Photonics /Plasmonics  Robots Robotic Metamolecule beacons: Hybridized robotic probes that are used in a realtime targeting of your DNA using florescent dyes.
Robotic AU NR Walkers:Robots that insert synthetic DNAbased motors into your body.
Robotic Nanoclocks: A shapeshifting flexible or “metamorphic” nanodevice, independently controllable elements, that can rotateenlarging or contracting the total surface area of the device, with or without altering the enclosed volume of the entire nanomachine. It maintains the structural integrity of the hydrogel away from your soon to be dead body.
External Field Driven Robots Robotic arms and claws: Robots with arms and claws deployed into your body to grab whatever they are told to seize and mangle.
Robotic Nanohinges:A robot that will hinge synthetic materials to your body until your body becomes one with it (fusing).Robotic Nanorotors: A robot that can change the spin of electrons and atoms in your body. Robotic Swimmers: Robots that either can move on solids or swim in fluids when exposed to a physical or chemical stimulus. Untethered smallscale swimmers, which include both smallscale robots and motors, are tiny architectures made of a single microor nanostructures. They will be sold to you as microscopic nanobots swimming around in our bloodstream monitoring our health, clearing debris and toxins and keeping us healthy from the inside out.
Autonomous Robots

Robotic Walkers/Motors: Tiny biological robots that “walk” on filaments in your body to deploy payloads. Robotic Rotary Apparatus: A robot that has an upper and a lower chamber. Think of this as a counterfeit heaven and hell in your body. The compartments are kept distinct while the hydrogel grows and takes over your body.

Interacting Dynamic Robotic Populations: Control task of robots interaction with a dynamic environment based on the stability of a closedloop control system, such as your immune system. Think of these as internal Slaughterbots. These are types of Robots that will crawl through your body when you take anything with hydrogel or quantum dot. These robots multiply and take over your body and turn you from a human into a synthetic entity. This does not include the following that will be included in the vaccine according to Rocky Mountain Laboratories, a NIH Lab in Hamilton, MT:

Aborted babies Humanized miceHumanized plantsSterilization chemical Drug cocktail to combat noncommunicable diseases such as obesity, heart disease, and diabetes CRISPR technologies. If you allow them in, you cannot get them out. What can you do? Say NO to anything with hydrogel or Quantum Dot.

This includes testing, vaccinations, and medications. You are the the Image Bearer and Ambassador of Jesus Christ. You cannot allow Legions of robots and strange images into your body.

Liquid Crystals In Vaccines To Turn People Into Zombies

Nearly three decades ago, a French doctor warned the world of “vaccines” that would contain liquid crystals that when exposed to magnetic frequencies would turn the recipients of those “vaccines” into “zombies.”

Dr. Pierre Gilbert is married and father of 4 children. He was born in Trois-Rivières Ouest, province of Quebec although he lived in the Bahamas and in the United States. In 1962, after a college course in science, he graduated from Palmer University in Davenport, Iowa USA as a chiropractor.

Among his experiences and qualifications, according to his website:


  • It has been in practice since 1962 and in 1974 established a system of seven clinics and operated up to 7 clinics at a time.
  • In 1978, he opened a fasting clinic in the Bahamas, on the island of Eleuthera, especially for heart patients.
  • In 1979 he joined a group of nutritionists under the auspices of the King Mountain Academy. These studies were based on “the biochemical balance of saliva and urine”.
  • Dr Gilbert is the author of written chronicles and of a book entitled “La Santé Totale”.


  • In 1974, he created Health Seminars, both for the profession and for the public. He was a consultant for one of the largest such firms in the US.
  • He was a member of various research societies such as: American Arthritic Society Gonsted Technics, Goodhearth Kinesiological Research Group, Van Rumpt Reflex Technic.

Dr. Gilbert stated, “The vaccines will have

liquid crystals that will be come hosted in the brain cells, which will become micro-receivers of electromagnetic fields where waves of very low frequencies will be sent.”

“And through these low frequency waves, people will be unable to think, you’ll be turned into a zombie,” he continued.

“Don’t think of this as a hypothesis,” he added. “This has been done. Think of Rwanda.”

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Here’s the video.

In 2016, researchers at the University of Virginia in Charlottesville genetically engineered a magnetized protein, called Magneto, which is inserted into a virus that’s injected into an animal’s brain to manipulate neural activity under the remote influence of magnetic fields….

Neuroscientist Steve Ramirez of Harvard University, left, who uses optogenetics to manipulate memories in the brains of mice, says the mind control study is “badass”.

“Previous attempts [using magnets to control neuronal activity] needed multiple components for the system to work – injecting magnetic particles, injecting a virus that expresses a heat-sensitive channel, [or] head-fixing the animal so that a coil could induce changes in magnetism,” he explains. “The problem with having a multi-component system is that there’s so much room for each individual piece to break down.”

This remarkable study is notable given anecdotally reported strange side effects with the COVID-19 vaccine involving magnetism.

It’s also worth pointing out that Canadian theology professor Dr. Pierre Gilbert (above) during a lecture in 1995 warned of a coming mandatory vaccine containing liquid crystals that, when exposed to magnetic frequencies, turn vaccine recipients into “zombies.”

“In the biological destruction there are the organized tempests on the magnetic fields,” Gilbert said. “What will follow is a contamination of the bloodstreams of mankind, creating intentional infections.”

“This will be enforced via laws that will make vaccination mandatory,” he continued. “And these vaccines will make possible to control people.”

Graphene Antennas Can Be Two Orders Of
Magnitude Smaller Than Metal Antennas
…Think Internal Nanotech Possibilities

Via Dr Leonard Coldwell
Note – The entire paper is in German on the pdf below.
Graphene antennas can be up to two orders of magnitude smaller than metallic antennas at the same resonant frequency.
The integration of graphene antennas into integrated circuits is therefore ideally suited to realize on-chip communication and thus increase computing power.
The research description realization and investigation of these antennas is the content of this thesis.


Here is the Abstract only in English…


Today’s digitalization is largely made possible by connecting digital components and increasing computing power. This has led to applications and research in the last decades that were previously not possible due to the lack of computing power. These include autonomous driving, deep learning and artificial intelligence. The constant technical progress described by Moore’s Law can be traced back to the miniaturiza- tion of components such as transistors. This increases the density of transistors on a processor core and thus its computing power.

However, further compliance with Moore’s Law and thus digital progress cannot be achieved in the future by reducing the size of the components alone. Already today, fundamental physical limits are being reached, such as heat dissipation, which make further miniaturization very difficult. Therefore, alternatives are needed to further increase computing power in the future.

One possibility is massive parallelization. Here hundreds to thousands of cores are connected in parallel to increase the compu- ting power. However, classical on-chip communication methods such as BUS systems are unsuitable for communication between the cores, as they are only scalable to a limited extent. An alternative is wireless communication, as a key technology for complex architectures.

In addition to scalability, this communication technology also has the possibility of reconfiguration and adaptation to current requirements and is therefore perfectly suited for agile network architectures. For this purpose, each core requires an antenna to send signals and receive signals from other cores.

The size of the antenna plays a decisive role here, because miniaturization has made the space on a core very precious. Classical metal antennas emitting at one THz have a length of approximately 7000 transistor channels and are therefore far too large.

With graphene, on the other hand, there is a fundamentally altered relationship bet- ween antenna length and resonance frequency due to the unique material properties. This means that graphene antennas can be up to two orders of magnitude smaller than metallic antennas at the same resonant frequency. The integration of graphene antennas into integrated circuits is therefore ideally suited to realize on-chip commu- nication and thus increase computing power. The research, description, realization and investigation of these antennas is the content of this thesis.

The introduction is followed by the theoretical principles for the description of these antennas. Here, first some important antenna fundamentals are explained and then the fundamental descriptions of plasmons are presented. This is followed by a description of graphene. The chapter concludes with the theoretical treatment of plasmonic graphene antennas.

After considering the current state of research, the measuring and manufacturing methods are explained. First of all, lithography, which is used to manufacture theantenna structure, is discussed. The next point is the description of the TDS measurement setup used to measure the antennas.

Next, theoretical considerations and calculations on the material requirements of graphene follow. The length of the antenna is of crucial importance. Here it is shown that for a functional graphene antenna a good match between antenna geometry and material quality is required.

During the technological realization, after some challenges, a stable manufacturing process could be established. For the characterization of graphene different methods are considered. For this purpose needle measurements on the SEM, TDS transmission measurements and Raman spectroscopy are suitable.

After the production and characterization of graphene, the dipole antennas are mea- sured in the TDS test setup. The first measurements show that, in addition to the antenna effect, charge carriers accelerated by an electrical bias voltage also contribute to the THz emission.

To minimize the influence of this effect, antennas were manufactured and measured in an alternative geometry (H-structure). A clear influence of graphene on the amplitude of the emitted THz radiation was found. The origin of this signal is the concentration of the electric field created by the bias voltage between the antenna arms. These measurements show the first THz emission of a graphene antenna structure.

In order to increase the material quality, samples were produced where either one or both sides of the graphene antenna are covered with hBN. Measurements on these antennas show a significantly increased THz emission due to the concentration of the electric field between the two antenna arms.

Finally, various possibilities to increase the emission of the graphene antenna are presented. There are possibilities to change the sample setup and geometry as well as external influences like doping and temperature

The final conclusion is followed by a critical discussion of the theoretical and practical results of this work and a classification into possible fields of research and application. This work shows the first THz emission of a graphene antenna structure and provi- des detailed theoretical, technological and experimental results, which are needed to realize a functional graphene antenna.